search
Back to results

Nutrition Intervention Among Stem Cell Recipients: Post Hospital Discharge

Primary Purpose

Hematopoietic Stem Cell Transplantation, Malnutrition

Status
Completed
Phase
Not Applicable
Locations
Lebanon
Study Type
Interventional
Intervention
Nutrition Intervention
Sponsored by
American University of Beirut Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hematopoietic Stem Cell Transplantation

Eligibility Criteria

16 Years - 80 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults admitted to the adult BMT service at AUBMC
  • Allogeneic or autologous SCT
  • Malignant or non-malignant indication for SCT

Exclusion Criteria:

  • Patients who pass away before day +100
  • Patients who miss 2 assessment points

Sites / Locations

  • American University of Beirut Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Nutrition Intervention Group

Arm Description

Upon discharge from the medical center, patients would be advised on a qualitative, neutropenic diet. Participants' quality of life, physical activity level, functional and nutritional status would be assessed at days +30, +60 and +100 post transplantation. These participants will not receive nutritional counseling by the dietitian as outpatients except if referred by the medical team.

Upon discharge from the medical center, NIG patients will receive tailored nutrition counseling with the provision of patient education material and oral nutritional supplements if needed. Patients will be advised on a diet high in energy and proteins and tailored to their medical condition in the hospital before discharge. Patients will be followed up at days +30, +60 and +100 post transplantation. Compliance will be measured at each visit by comparing patients caloric and protein needs to their actual protein and energy intake. Compliance will be reinforced to meet patients' goals using nutritional tips, oral supplementation, and artificial nutrition use.

Outcomes

Primary Outcome Measures

Proportion of patients with a PGSGA score ≥4

Secondary Outcome Measures

Handgrip strength
Lean Body Mass Changes
Re-hospitalization Rate
Quality of life (QoL) [ Time Frame: 100 days post transplantation ]

Full Information

First Posted
June 1, 2016
Last Updated
February 7, 2018
Sponsor
American University of Beirut Medical Center
Collaborators
Aix Marseille Université
search

1. Study Identification

Unique Protocol Identification Number
NCT02791347
Brief Title
Nutrition Intervention Among Stem Cell Recipients: Post Hospital Discharge
Official Title
Nutrition Intervention Among Stem Cell Recipients: a Randomized Controlled Trial Post Hospital Discharge
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
August 2016 (Actual)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
American University of Beirut Medical Center
Collaborators
Aix Marseille Université

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chemotherapy conditioning, preceding Stem Cell Transplantation (SCT), has been associated with severe gastrointestinal toxicity, commonly compromising patients' food intake, nutritional status and functioning level. Malnutrition has been associated with worse functional status, reduced survival, increased rate of infections, complications, hospitalizations, and therapy toxicity in oncology patients. To date, there is no Randomized Controlled Trials (RCT) assessing the impact of a nutrition intervention on SCT patients who remain at risk of malnutrition even 100 days post SCT. The proposed study is a single center, prospective, RCT with a parallel design that aims to assess the impact of a nutrition intervention on the nutritional and functional statuses of SCT recipients 100 days post SCT.
Detailed Description
This study is a single center RCT with a parallel design. It aims to improve the SCT recipients' nutritional status and QoL and reduce the associated morbidities. Results of the study can guide the recommendations for the medical and nutritional outpatient assessment post SCT. During the pre-SCT workup, patients will be invited to participate in the study. Around discharge from the hospital, recruited patients will be randomized to a control or an intervention group based on permuted block random sampling. Patients in the Nutrition Intervention group (NIG) will receive a tailored diet plan from the dietitian as well as regular outpatient follow-ups measuring and reinforcing compliance. Patients in the Control Group (CG) will receive usual care; they will only be assessed in the nutrition clinics upon referral by the medical team. The body composition, Quality of Life (QoL), Physical Activity (PA) level, nutrient intake, functional status and nutritional status of both groups will be evaluated at regular intervals during the hospital stay and post discharge through the Patient Generated Subjective Global Assessment (PGSGA), Body Impedance Analysis (BIA), handgrip strength, Functional Assessment of Cancer Therapy -Bone Marrow Transplantation (FACT-BMT), PA questionnaire and Karnofsky scale. Moreover, patients' food intake will be analyzed for its micronutrient and macronutrient content to assess the changes in nutrient analysis in the peri-transplantation phase. When applicable, BIA and Computed Tomography (CT) tests will be compared for their agreements. Considering a power of 80%, an attrition rate of 30% and a difference of 40% between the NIG and CG groups, 52 patients need to be recruited in the study. Analysis will be done based on 'intention to treat' and 'per protocol' analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hematopoietic Stem Cell Transplantation, Malnutrition

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Upon discharge from the medical center, patients would be advised on a qualitative, neutropenic diet. Participants' quality of life, physical activity level, functional and nutritional status would be assessed at days +30, +60 and +100 post transplantation. These participants will not receive nutritional counseling by the dietitian as outpatients except if referred by the medical team.
Arm Title
Nutrition Intervention Group
Arm Type
Experimental
Arm Description
Upon discharge from the medical center, NIG patients will receive tailored nutrition counseling with the provision of patient education material and oral nutritional supplements if needed. Patients will be advised on a diet high in energy and proteins and tailored to their medical condition in the hospital before discharge. Patients will be followed up at days +30, +60 and +100 post transplantation. Compliance will be measured at each visit by comparing patients caloric and protein needs to their actual protein and energy intake. Compliance will be reinforced to meet patients' goals using nutritional tips, oral supplementation, and artificial nutrition use.
Intervention Type
Other
Intervention Name(s)
Nutrition Intervention
Primary Outcome Measure Information:
Title
Proportion of patients with a PGSGA score ≥4
Time Frame
100 days post transplantation
Secondary Outcome Measure Information:
Title
Handgrip strength
Time Frame
100 days post transplantation
Title
Lean Body Mass Changes
Time Frame
100 days post transplantation
Title
Re-hospitalization Rate
Time Frame
100 days post transplantation
Title
Quality of life (QoL) [ Time Frame: 100 days post transplantation ]
Time Frame
100 days post transplantation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults admitted to the adult BMT service at AUBMC Allogeneic or autologous SCT Malignant or non-malignant indication for SCT Exclusion Criteria: Patients who pass away before day +100 Patients who miss 2 assessment points
Facility Information:
Facility Name
American University of Beirut Medical Center
City
Beirut
Country
Lebanon

12. IPD Sharing Statement

Learn more about this trial

Nutrition Intervention Among Stem Cell Recipients: Post Hospital Discharge

We'll reach out to this number within 24 hrs